Specialty coordination
Bring the proposed investigator, local practice, and procedure partners into the same preparation process.
Gastroenterology clinical research
Gastroenterology Clinical Trial Sites and Research Support
Digestive-disease research starts with the right clinical connections.
Clinical fit and patient access
Digestive-disease research starts with the right clinical connections.
Gastroenterology protocols connect office-based care with procedures, symptom reporting, specimen collection, and long-term follow-up. WGR brings these needs into one feasibility discussion. Through our sister company Wellness Clinical Research and participating practice relationships, we assess digestive-disease opportunities in South Florida and Puerto Rico, with the proposed investigator and procedure pathway reviewed for each study.
Existing clinical relationships provide context that a simple diagnosis count cannot. Our assessment distinguishes available records from people who may meet the study’s treatment, disease-activity, and procedural requirements. Local and central teams agree on a practical outreach and follow-up plan before recruitment commitments are made.
Conditions and program types
A starting point for
protocol-specific review.
These examples describe the kinds of populations and indications that can inform a feasibility discussion. They are not a list of currently enrolling studies.
From clinical fit to coordinated execution
The operational detail
behind the indication.
Sample workflows
Plan collection, processing, temperature requirements, shipment, and protocol-specific documentation.
Central recruitment
Coordinate records-based outreach, prescreening, referral follow-up, and screening arrangements through WGR’s in-house team.
Study continuity
Connect visit preparation with regulatory, monitoring, quality, and financial follow-through throughout execution.
For sponsors & CROs
Gastroenterology study
needs enrollment support?
For a gastroenterology trial needing enrollment recovery, we review where the pathway is breaking down: identifying the right disease population, obtaining records, arranging procedures, or completing screening. A proposed rescue plan ties the actual barrier to available investigators, patient access, procedure capacity, and the time remaining in the study.
Review the pathway
before the next commitment.
Connect indication-specific feasibility with our in-house recruitment team and local clinical review. The recovery scope depends on available resources and the remaining study requirements.
Discuss a rescue studyExplore trial rescueStudy planning questions
A useful first
conversation.
Can WGR coordinate endoscopy requirements?
We assess the proposed location’s procedure relationships, scheduling, specimen needs, and documentation requirements during feasibility. Procedure availability is confirmed for the individual protocol.
How do you assess an IBD recruitment estimate?
The review considers diagnosis, treatment history, disease activity, prior testing, competing studies, and screening burden. Access to records is a starting point, not confirmation of eligibility.
What should a sponsor send for an initial GI review?
A synopsis or protocol, key eligibility criteria, required procedures, location preferences, and enrollment timelines help us identify the right clinical and operational reviewers.
Related clinical expertise
Connected therapeutic areas.
Connect with what comes next
Let’s build research
around your strengths.
A medical practice. A study opportunity. A shared ambition.